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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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p-Methoxyphenylthionophosphine sulfide → Benzo-1,2,3-thiadiazole-7-thiocarboxamide

HRID 483971
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인쇄 미리보기

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HRID 483971 반응식
COC1C=CC(P(=S)=[S:10])=CC=1.[S:12]1[C:16]2[C:17]([C:21]([NH2:23])=O)=[CH:18][CH:19]=[CH:20][C:15]=2[N:14]=[N:13]1>C1(C)C=CC=CC=1>[S:12]1[C:16]2[C:17]([C:21](=[S:10])[NH2:23])=[CH:18][CH:19]=[CH:20][C:15]=2[N:14]=[N:13]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 16162075p-Methoxyphenylthionophosphine sulfideHCID 22403364Benzo-1,2,3-thiadiazole-7-carboxylic acid amide

생성물 1

HCID 19088000Benzo-1,2,3-thiadiazole-7-thiocarboxamide수율 56.4%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A suspension of 2.42 g of p-methoxyphenylthiono-phosphine sulfide and 1.79 g of benzo-1,2,3-thiadiazole-7-carboxamide in 95 ml of toluene is refluxed under a nitrogen atmosphere for 6 hours. The mixture is then evaporated in vacuon and the residue is suspended in ethyl acetate and filtered off. The filtrate is recrystallized from ethyl acetate/tetrahydrofuran with added active charcoal. 1.1 g of yellow crystals of melting point 129°-131° C. result.

후처리

  1. temperatureis refluxed under a nitrogen atmosphere for 6 hours
  2. customThe mixture is then evaporated in vacuon
  3. filtrationfiltered off
  4. customThe filtrate is recrystallized from ethyl acetate/tetrahydrofuran
  5. additionwith added active charcoal

출처 및 근거

ORD 기록
ord-ed276ae7cf7e46749d6f50b6ed188934
출처 데이터셋
uspto-grants-1993_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05229384

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